Your specialist in Quality and Compliance Management within Life Science.
The complex rules of our regulated industry are changing constantly. Your business needs to keep up with that change to be compliant, and deliver quality. Let us guide you.
Q-People provides targeted solutions in Quality and Compliance projects in the Life Sciences sector, from Pharmaceutical and Biotech to API and Medical Device Production.
What we do
Q-People helps companies to set up and support Quality and Compliance processes, procedures and systems. Training, mentoring and coaching of talent within the Life Sciences sector is our strength. We don’t want specialist knowledge or talent to go to waste.
Every quality process requires an approach tailored to the specific needs of the production environment. We map out the current situation in accordance with the latest legislation.
Through validation and controlling quality risks we guarantee that your company complies with regulations and product safety is guaranteed.
meet our satisfied customers
Domains of expertise
We offer support and knowledge in all domains of Quality and CGMP Compliance Management.
- Design and development of quality management systems
- Assistance in defining compliancy strategies
- Validation Processes, software and equipment
- Control of quality risks
- Preparation of quality and compliance audits
- Are educated and committed people who will bring added-value
- Have a background in the Life Sciences sector
- Are uniquely skilled, to cover the Full Quality Management System
- Will continuously be trained and certified
- Guarantee a powerful level of engagement
Meet our Q-Experts
Half of all safety warnings issued to drug manufacturers in India and ChinaHalf of all safety warnings issued to drug manufacturers in India and China... From early 2018 until August 2019, the FDA’s Office of Manufacturing Quality has published 18 warning letters to pharmaceutical manufacturers in China and 19 warning letters to facilities in India. Read more in this article about the concerns.
Q-Academy: Open training Sessies Q4-2019Hierbij een overzicht van de komende training sessies van onze Q-Academy voor Q4-2019. Onze opleidingen binnen onze Q-Academy zijn "gratis" beschikbaar via Co-valent: Co-valent biedt GRATIS opleidingen aan voor ondernemingen die behoren tot de life science sector - paritair comité 116 (arbeiders) of 207 (bedienden). - 25 Oktober 2019: DAG 2 - Advanced cGMP & QMS (Niel) : https://www.co-valent.be/nl/details-formations/?sja=5744b10eZff5fZe811Zba26Z005056b04a46 - 16, 17 & 18 December 2019: DAG 1 - Contaminatie controle in cleanrooms - Algemeen (Niel) : https://www.co-valent.be/nl/details-formations/?sja=f3fbcf6fZd1ecZe811Za958Z005056b04a46 DAG 2 - Contaminatie controle in cleanrooms - Contaminatie Controle Grade D+C (Niel): https://www.co-valent.be/nl/details-formations/?sja=f3fbcf6fZd1ecZe811Za958Z005056b04a46 DAG 3 - Contaminatie controle in cleanrooms - Contaminatie Controle Grade A+ B Niel: https://www.co-valent.be/nl/details-formations/?sja=6bb579bfZ3e7dZe911Za966Z000d3a29fb7a - 21 November 2019: DAG 1 : Basis in Equipment & System qualification (Niel) : https://www.co-valent.be/nl/details-formations/?sja=b9ef8c5dZfd5fZe811Zba26Z005056b04a46 - 22 November 2019: DAG2 : Vervolg Equipment & System qualification (Niel) : https://www.co-valent.be/nl/details-formations/?sja=deaeb6f5Zb178Ze911Za96aZ000d3a29f080 - 25 November 2019: Technical writing : behandelen van deviaties (Geel) : https://www.co-valent.be/nl/details-formations/?sja=704fadd0Zb278Ze911Za96aZ000d3a29f080 - 2 December 2019 GLP labo activiteiten in Life Sciences (Niel) : https://www.co-valent.be/nl/details-formations/?sja=24c2af87Zaf78Ze911Za96aZ000d3a29f080 - 9 December 2019 Technical writing : behandelen van deviaties (Niel) : https://www.co-valent.be/nl/details-formations/?sja=704fadd0Zb278Ze911Za96aZ000d3a29f080
AQbD, the Evolution of Pharmacopoeial Standards?At Q-People we are actively acting on the constant change… Expectation on expertise level is becoming higher, and skills sets are changing to deliver qualitative medicines in a more efficient way. Composing the wright skill sets in the future, will have a positive impact on “Time to Market”. In this article you can read more about new insights were expertise is needed at early stages of Quality Control processes.
October 25 @ 8:30 am – 5:00 pm
November 21 @ 8:30 am – 5:00 pm
November 22 @ 8:30 am – 5:00 pm
November 25 @ 8:30 am – 5:00 pm
December 2 @ 8:30 am – 5:00 pm